A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption
- PMID: 15795603
- DOI: 10.1097/01.mpg.0000153097.73083.a3
A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption
Similar articles
-
A missense mutation in the Na(+)/glucose cotransporter gene SGLT1 in a patient with congenital glucose-galactose malabsorption: normal trafficking but inactivation of the mutant protein.Biochim Biophys Acta. 2001 May 31;1536(2-3):141-7. doi: 10.1016/s0925-4439(01)00043-6. Biochim Biophys Acta. 2001. PMID: 11406349
-
Molecular basis for glucose-galactose malabsorption.Cell Biochem Biophys. 2002;36(2-3):115-21. doi: 10.1385/CBB:36:2-3:115. Cell Biochem Biophys. 2002. PMID: 12139397 Review.
-
Congenital Glucose-Galactose Malabsorption in a Turkish Newborn: A Novel Mutation of Na+/Glucose Cotransporter Gene.Dig Dis Sci. 2017 Jan;62(1):280-281. doi: 10.1007/s10620-016-4348-2. Epub 2016 Oct 25. Dig Dis Sci. 2017. PMID: 27783308 No abstract available.
-
I. Glucose galactose malabsorption.Am J Physiol. 1998 Nov;275(5):G879-82. doi: 10.1152/ajpgi.1998.275.5.G879. Am J Physiol. 1998. PMID: 9815014 Review.
-
[Selective congenital glucose, galactose malabsorption in the small intestine].Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):552-4. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9645131 Review. Japanese. No abstract available.
Cited by
-
Fructose Metabolism and Its Effect on Glucose-Galactose Malabsorption Patients: A Literature Review.Diagnostics (Basel). 2023 Jan 12;13(2):294. doi: 10.3390/diagnostics13020294. Diagnostics (Basel). 2023. PMID: 36673104 Free PMC article. Review.
-
Congenital glucose-galactose malabsorption: a novel deletion within the SLC5A1 gene.Eur J Pediatr. 2013 Mar;172(3):409-11. doi: 10.1007/s00431-012-1802-9. Epub 2012 Jul 29. Eur J Pediatr. 2013. PMID: 22843301
-
Nephrocalcinosis in glucose-galactose malabsorption: nephrocalcinosis and proximal tubular dysfunction in a young infant with a novel mutation of SGLT1.Eur J Pediatr. 2008 Dec;167(12):1395-8. doi: 10.1007/s00431-008-0681-6. Epub 2008 Feb 21. Eur J Pediatr. 2008. PMID: 18288487
-
Diagnosing and Treating Intolerance to Carbohydrates in Children.Nutrients. 2016 Mar 10;8(3):157. doi: 10.3390/nu8030157. Nutrients. 2016. PMID: 26978392 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical